XMAP215, Dis1, TOG
microtubule plus end binding protein - stimulates microtubule growth, microtubule destabilising activity, mitotic spindle
Please see the JBrowse view of Dmel\msps for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Gene model reviewed during 5.47
Interacts with tacc, dgt6 (PubMed:11433295, PubMed:19836241). Interacts with mv (PubMed:33725482). Interacts with Patronin (PubMed:32066907).
The TOG (tumor overexpressed gene) domains are arranged in a N-terminal pentameric array with each domain composed of six (for the most part non-canonical) HEAT repeats forming a oblong paddle-like structure. Intra-HEAT loops are positioned along a face of the TOG domain and bind to a single alpha/beta-tubulin heterodimer. The TOG domains in the array seem to be structurally and functionally polarized. Differential functions may range from microtubule (MT) lattice binding and/or free tubulin heterodimer binding to potentiating stable incorporation of tubulin into the MT lattice. TOG 1-2 show strong and TOG 3-4 weak tubulin binding; TOG 1-5 are required for full ability to promote MT polymerization.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\msps using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
Comment: maternally deposited
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
msps is expressed throughout oogenesis, in both germ cells and follicle cells. In young egg chambers, msps mRNA accumulates in oocytes. At oogenesis stages 8-9, msps mRNA is localized to the anterior cell cortes in oocytes. Expression increases at stage 10, and mRNA is evenly distributed in late-stage (stage 12-14) oocytes.
JBrowse - Visual display of RNA-Seq signals
View Dmel\msps in JBrowse3-58
3-57.9
Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete
Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.
For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.
polyclonal
S2 cells treated with RNAi against msps show reduced poleward flux rates of tubulin subunits in mitotic spindles and sharply decreased α-tubulin turnover at the microtubule plus and minus ends of the spindles. There is a significantly increased scatter of chromosomes throughout the spindle in the RNAi treated cells compared to controls. Pole-to-pole spindle lengths are significantly reduced in the RNAi treated cells compared to controls.
RNAi screen using dsRNA made from templates generated with primers directed against this gene results in aberrantly short spindles when assayed in S2 cells. This phenotype can be observed when the screen is performed with or without Cdc27 dsRNA.
S2 cells transfected with dsRNA made from templates generated with primers directed against this gene show shortening of the metaphase spindle.
msps is required during oogenesis for the normal structure and function of cytoplasmic microtubules.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
msps is required for the integrity of the mitotic spindle.
Mutation in msps disrupts the integrity of the mitotic spindle, resulting in the formation of one or more small additional spindles in diploid cells.
Source for merge of: msps anon-WO0140519.136
Source for merge of msps anon-WO0140519.136 was sequence comparison ( date:051113 ).